FDA Import Refusal 799-5135593-7/1/1 — Philips North America, LLC

Philips North America, LLC — FEI 1218950

The FDA refused shipment 799-5135593-7/1/1 from Philips North America, LLC (United States) on April 15, 2016. The refused product falls under Devices — NEBULIZER (DIRECT PATIENT INTERFACE). Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.